CA3087901C - Temperature-resistant silicone resins - Google Patents

Abstract

Methods and formulations for modified silicone resins of Formula (I) are presented: (See Formula I) The R1, R2, and R3 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl; n ranges from 1 to 10; m ranges from 1 to 200; and p ranges from 2 to 1,000. The elastomeric materials prepared from modified silicone resins display robust mechanical properties following prolonged exposure to high temperatures (e.g., 316°C or higher).

Description

TEMPERATURE-RESISTANT SILICONE RESINS
FIELD
The disclosure relates generally to methods and formulations for high temperature-resistant silicone resins.
BACKGROUND
A critical need exists for elastomers capable of performing in extreme themtal environments. Silicone polymers represent a group of elastomers owing to their inherent thelmal and oxidative stabilities. Silphenylene siloxane polymers are known to be stable at high temperatures. This is due in part to the presence of the rigid silphenylene moiety that interferes with the siloxane redistribution reaction. Silphenylene siloxane polymers have been synthesized and investigated by several research groups over the past several decades (see, for example. Dvomic, P. R.; Lenz, R. W. High-Temperature Siloxane Elastomers:
Huethig &
Wepf Verlag: New York, 1990).
For example, Hundley and Patterson (N.H. Hundley and W.J. Patterson, "Formulation/Cure Technology for Ultra-High Molecular Weight Siphenylene-Siloxane Polymers" NASA Technical Paper 2476 (1985)) studied certain derivatives of silphenylene-siloxane (SPS) polymers having the formula shown below:
H
I
tin The main obstacle to use of these polymers and related carborane derivatives is their inability to be easily vulcanized to effect curing. Hundley and Patterson prepared derivatives of SPS
polymers, wherein a vinyl group substituent replaced a methyl substituent, giving the modified SPS polymer formula shown below:

Date Recue/Date Received 2020-07-24 tr 1114 1 1 Si The inclusion of the vinyl substitucnt in such SPS polymer derivatives considerably improved curing by vulcanization. Importantly, such SPS polymer derivatives demonstrated improved thermal and oxidative stabilities over extant commercial silicone resin polymer formulations. Yet both elastomer formulations exhibited extensive degradation in mechanical properties after being exposed to 288 C for 16 hr. (Id. at p. 10).
MacKnight and coworkers (U. Laufer et al. "Vinyl-Substituted Silphenylcne Siloxane Copolymers: Novel High-Temperature Elastomers" Macromolecules 32, 3426-3431 (1999)) prepared and studied SPS polymer formulations that included 30-70 percent vinyl .. substitution as depicted by one exemplary fonnula shown below:
tr I ID I
Si I I
While these derivatives displayed greater thermal stability than prior formulations, the high temperature limit for possible applications of these materials as fire-safe elastomers extends to about 230 'V
Homrighausen and Keller (CL. Homrighausen and T.M. Keller, "High-Temperature Elastomers from Silarylene-Siloxane- Diacety-lene Linear Polymers," J. Polym.
Sci. Part A:
Polym. Chem. 40:88-94 (2002)) prepared and characterized linear silarylene-siloxane-diacetylenc polymers having the formula shown below:
Date Recue/Date Received 2020-07-24 I I I I I I I
___________________ Si-o si m si-o-(si-o si jot Si-0) jrn I I I W I I I WI I
where n = 1-3. Polymers that contain the vulcanizable acetylene moiety as part of the chain or as a pendant functional group are known in the art. In most cases, incorporation of the acetylene group improves the thermal stability of the respective polymers. The increase in thermal stability is believed to be due to generation of a cross-linked material. Yet elastomers based upon these polymers began to exhibit significant weight loss after a couple of hours at temperatures up to about 330 C in air as determined by thermogravimetric analysis (TGA, Id.).
Additional compounds include those having phosphorous as a substituent, for example:
1101 Poly[oxy(dimethylsilylene)], a,et--(phenyl- phosphinylidene)bisko-hydroxy-] (CAS 1342156-21-1) HO Si 0 P 0 3i CH
- 1 n 11 - n 01 ---- Poly[oxy[(2-chloro ethyl)-[

n phosphinylidcne]oxy(1,1,3,3-tetramethyl-1,3-disiloxanediy1)]
0¨P ¨O¨Si----0¨Si (9CI) (CAS 738622-48-5) 1 Phosphonic acid, (4-ethenylpheny1)-, n-Bu ' butoxydimethylsilyl methyl ester 0 0 (9CI) (CAS 151543-47-4) ¨SI¨O¨P
II \

Date Recue/Date Received 2020-07-24 o./ Phosphonic acid, dimethylsilylene 0 dimethyl ester (9CI) (CAS 125789-I 1 09-5) HP¨O--Si---O---PH

Poly[oxyphosphinylideneoxy-' (dimethylsilylene)-oxyphosphinylideneoxy(methylphen yl-silylene)] (9CI) (CAS 134027-33-1) [ _ 0 Pi 0 si 0 r . si 1 1 1 I _ n 41) Phosphonic acid, vinyl-, bimol cyclic diphenylsilylene ester, polymers (8CI) (CAS 29797-84-0) 63.-0 P-----...
0 \------ 0 ,NP-----n -----...õ, I Phosphonic acid, vinyl-, bimol.
cyclic dimcthylsilylene ester, C\ õ7"------P----_ polymers (8CI) (CAS 29797-83-9) o __ \----0 I // " õ/NP.----0-7 =/0 1 i Date Recue/Date Received 2020-07-24 S Phosphonic acid, ethenyl-, diphenylsilylene ester, homopolymer (9CI) (CAS 29797-82-8) OH OH Phosphonic acid, vinyl-, dimethylsilylene ester, polymers ¨ 0¨Si¨ O¨P (8CI) (CAS 29797-81-7) Most elastomeric polymers containing these species are also sensitive to thermal degradation. For example, the first structure in the table (CAS 1342156-21-1) was used in the preparation of polyester resins but their decomposition temperatures (5%
weight loss T5%) are all below 300 C, rendering them ill-suited for long-term use at such temperatures.
Commercially available silicone-based elastomeric materials, such as that exemplified by room temperature vulcanized 60 ("RTV60"), lose their mechanical properties as they decompose at operating temperatures (for example, 316 C) for a relatively short life span (for example, a few hundred hours). Thus, there is still a need for elastomeric materials having .. improved temperature stability, longevity and robust mechanical performance for prolonged periods of time at high temperatures.

Date Recue/Date Received 2020-07-24 BRIEF SUMMARY
In a first respect, a modified silicone resin of Formula (I) is disclosed:

HO ______________________ Si ((0 __ P)(0 ___ Si) \I OH
Mn rnip wherein RI, R2, and R3 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl; n ranges from 1 to 10; m ranges from 1 to 200; and p ranges from

2 to 1,000.
In a second respect, an elastomer formulation is disclosed. The elastomer formulation includes at least one modified silicone resin of Formula (I):

HO __________________ Si ((0 __ P)(0 __ Si)m) OH
In R2 0 R2 (I) wherein R', R2, and R3 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl; n ranges from 1 to 10; m ranges from 1 to 200; p ranges from 2 to 1,000; and at least one metal oxide. The elastomer formulation may further include at least one curing agent.
In one embodiment, there is provided a modified silicone resin of Formula (I).

HO¨Si ______________________ ((0 P)(0 SiL) OH
n R2 0 R2 (I) RI, R2, and R3 may each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl, n ranges from 1 to 10, m ranges from 1 to 200, and p ranges from 2 to 1,000.

Date Recue/Date Received 2020-07-24 The modified silicone resin may range from m ranges from 1 to 100; and p ranges from 10 to 500.
R', R2, and R3 may each independently selected from a group consisting of II, Ci_g alkyl, C2_8 alkenyl, C2-8 alkynyl, and aryl.
RI, R2, and R3 may each independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl, and aryl.
R2, and R3 may each independently selected from a group consisting of methyl, phenyl, and vinyl.
The modified silicone resin may be selected from a group consisting of:
(i) HO¨Si ((0¨P) (0¨Si)n) OH
n P

(ii) HO¨Si ((0¨P) (0¨Si)m) OH
n (iii) HO¨Si ((0¨P) (SO¨Si)) OH
n (iv) HO¨Si ((0¨P) (0¨Si)) OH
n Date Recue/Date Received 2020-07-24 (v) HO Si ((0 P) (0¨Si)m) OH
n (vii) HO Si ((0 P) (0¨Si)n) OH
n P

(viii) HO¨Si ((0¨P) (0¨Si) \ OH
n n4 n ranges from 1 to 10, m ranges from 5 to 100, and p ranges from 10 to 500.
Values for n, m and p may provide a compound of Formula (I) having a viscosity ranging from about 500 cSt to about 10,000 cSt.
Ratio of n to m may range from about 1:1 to about 1:200.
In another embodiment, there is provided an elastomer formulation. The formulation includes at least one modified silicone resin of Formula (I) HO¨Si ((0 P) ( 0 Si)n) OH
n I p (1) Date Recue/Date Received 2020-07-24 RI, R2, and R3 may each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl. n ranges from 1 to 10, m ranges from 1 to 200, and p ranges from 2 to 1,000, at least one metal oxide, and at least one curing agent.
n may range from 1 to 3, m may range from 1 to 100, and p ranges from 10 to 500.
R, R2, and R3 may each independently selected from a group consisting of H, C1_8 alkyl, C2-8 alkenyl, C2-8 alkynyl, and aryl.
RI, R2, and R3 may each independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylcnyl, acetylenyl, diacctylenyl, and aryl.
RI, R2, and R3 may each independently selected from a group consisting of methyl, phenyl, and vinyl.
The at least one modified silicone resin may include at least one of the following:
(i) \
HO¨Si ((0¨P) (0¨Si) OH
n n-(13 (ii) HO¨Si (0¨P) (0¨Si) OH
n rr(p (iii) HO¨Si ((0¨P) (0¨SU OH
n Date Recue/Date Received 2020-07-24 (iv) HO¨Si ((0¨P) (0¨Si) OH
In rrip (v) HO¨Si ((0¨P) (0¨Si) \ OH
In m/p (vii) HO Si ((0 P) (0¨Si)n) OH
I n (viii) HO¨Si ((0 P) (0-3i) \ OH
n r113 n may range from 1 to 10, m may range from 5 to 100, and p may range from 10 to 500.
The at least one metal oxide may include at least one of iron oxide, titanium oxide, cerium oxide, zinc oxide, and zirconium oxide.
The at least one metal oxide may include at least one of iron oxide and titanium oxide.
The at least one metal oxide may have a particle diameter size ranging from about 1 nm to about 5 tim.
Date Recue/Date Received 2020-07-24 Values for n, m and p may provide a compound of Formula (I) having a viscosity ranging from about 500 cSt to about 10,000 cSt.
Ratio of n to in may range from about 1:1 to about 1:200.
The at least one modified silicone resin of Formula (I) may be present in an amount ranging from about 5 weight-percent to about 95 weight-percent, the at least one metal oxide may be present in an amount ranging from about 2 weight-percent to about 80 weight-percent.
The at least one curing agent may be present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.
At least one modified silicone resin of Formula (II), wherein Formula (II) may include at least one of each of the following subunits:
R8 R o _____________________________ 0 Si X Si 0 _____ 7d1 ___________________________________ \ 13)y.R and ( Si i ___________________________________ 0 )z R7 =
R6, R7, R8, R9, Rio, ¨11, R12 and R13 may each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl, X may be selected from a group consisting of arylene, transition metal, inorganic oxide, and silsesquioxane. t may range from 1 to 10, y may range from 1 to 200, and z ranges from 1 to 1,000.
t may range from 1 to 3, y may ranges from 1 to 100, and z may range from 10 to 500.

Date Recue/Date Received 2020-07-24 R6, R7, R8, R95 Rill, R11, N. ¨12, and R13 may each independently selected from a group consisting of H, Cl_g alkyl, Cmalkenyl, C2_8alkynyl, and aryl.
R65 R75 R8, R95 Rio, Rn, R'2, and R1.1 may each independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl, and aryl.
R6, R7, R8, R9, RH, R12, and R13 may each independently selected from a group consisting of methyl, phenyl, and vinyl.
The at least one modified silicone resin of Formula (I) may be present in an amount ranging from about 5 weight-percent to about 95 weight-percent. The at least one metal oxide may be present in an amount ranging from about 2 weight-percent to about 80 weight-percent, and the at least one curing agent is present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.
The elastomer formulation may include at least one of the following formulations:
Iron Curing Formula (I) Formula (II) Formulation # oxide agent I
(Y0 w/w) (% w/w) (Y0 w/w) ("A) w/w) 108 6 [Resin (i)] 49.5 [Resin (#2)1 44 0.5 111 5 [Resin (i)] 47 [Resin (#2)] 44 4 The iron oxide may include Fe2O3 having a particle size ranging from about 10 nm to about 5 [un. The curing agent may be at least one of dibutyltin dilaurate, tris(dimethylamino)methylsilane, and ethyltriacetoxysilane.
The elastomer formulation may include at least one silicate.
The at least one silicate may include at least one of ethyl silicate, methyl silicate, isopropyl silicate and butyl silicate.
The at least one modified silicone resin of Formula (I) may be present in an amount ranging from about 5 weight-percent to about 95 weight-percent. The at least one metal oxide may be present in an amount ranging from about 2 weight-percent to about 80 weight-percent.
The at least one silicate may be present in an amount ranging from 0 weight-percent to about Date Recue/Date Received 2020-07-24 25 weight-percent, and the at least one curing agent may be present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.
The elastomer formulation may include at least one of the following formulations:
Iron Ethyl Curing Formula (I) Formula (II) Formulation # oxide Silicate agent (% w/w) (% w/w) (0/0 w/w) (% w/w) (0/0 w/w) 104 8 [Resin (ii)] 45 [Resin (#2)] 44 2.5 0.5 105 7 [(Resin (i)] 46 [Resin (#2)] 44 2.5 0.5 The iron oxide may include Fe2O3 comprising a particle size ranging from about nm to about 5 lam, the curing agent may be at least one of dibutyltin dilaurate, tris(dimethylamino)methylsilane; and ethyltriacetoxysilane.
The elastomer formulation may include at least one silica.
The at least one silica may include at least one of fumed silica and functionalized silica.
The at least one modified silicone resin of Formula (I) may be present in an amount ranging from about 5 weight-percent to about 95 weight-percent, the at least one metal oxide may be present in an amount ranging from about 2 weight-percent to about 80 weight-percent.
The at least one silica may be present in an amount ranging from greater than 0 weight-percent to about 20 weight-percent. The at least one curing agent may be present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.
The elastomer formulation may include at least one silicate, and at least one silica.
The at least one silicate may include at least one of ethyl silicate, methyl silicate, isopropyl silicate and butyl silicate, and the at least one silica may include at least one of fumed silica and functionalized silica.
The at least one modified silicone resin of Formula (I) may be present in an amount ranging from about 5 weight-percent to about 95 weight-pereent, the at least one metal oxide may be present in an amount ranging from about 2 weight-percent to about 80 weight-percent, and the at least one silicate may be present in an amount ranging from 0 weight-percent to Date Recue/Date Received 2020-07-24 about 25 weight-percent. The at least one silica may be present in an amount ranging from greater than 0 weight-percent to about 20 weight-percent, and the at least one curing agent may be present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.
The elastomer formulation may be Iron Ethyl Curing Formula (I) Formula (II) Formulation # oxide Silicate agent (% w/w) (% w/w) (% w/w) (% w/w) (% w/w) 115 55.7 [Resin (i)] 6.55 [Resin 27.11 1.96 (Ethyl 0.54 (#2)] silicate);
8.14 (SiO2) The iron oxide may include Fe2O3 having a particle size ranging from about 0.5 gm to about 5 gm, and the curing agent may be at least one of dibutyltin dilaurate, tris(dimethylamino)methylsilane; and ethyltriacetoxysilane.
In one embodiment, there is provided a modified silicone resin that is the reaction product of:

HO-1- X-41-0 H HO ( Si 0 ________________________________ H

and Each of R6, R7, R8, R9, R111, and R1-1- is independently selected from the group consisting of H, alkyl, alkenyl, alkynyl, and aryl. X is an inorganic oxide, wherein the inorganic oxide is: a \
Ti ¨0/ \OH, wherein R21 cyclosiloxane, wherein the cyclosiloxane is not a silsesquioxane;

\Z( and R22 are independently propoxy, butoxy or phenyl; 2, wherein R23 and R24 are B\
independently propoxy, butoxy or phenyl; or , wherein R25 is propoxy, butoxy or phenyl. y ranges from 1 to 200.

Date Recue/Date Received 2021-09-01 In another embodiment, there is provided a method of forming modified silicone resin.
The method involves forming a reaction mixture by introducing into a reaction vessel a compound represented by formula (A):
R8. Fre HO-Si-- X-Si-OH

R9 Ri (A), and introducing into the reaction vessel a compound represented by formula (D):

HO ( Si 0 ____________________ H

(D).
Each of R6, R7, R8, R9, RI- , and R" is independently selected from the group consisting of H, alkyl, alkenyl, alkynyl, and aryl. X is an inorganic oxide, wherein the inorganic oxide is: a \
/Ti \OHcyclosiloxane, wherein the cyclosiloxane is not a silsesquioxane; , wherein R21 zr ____________________________________________________________________________ \oH10 and R22 are independently propoxy, butoxy or phenyl; , wherein R23 and R24 are independently propoxy, butoxy or phenyl; or , wherein R25 is propoxy, butoxy or phenyl. y ranges from 1 to 200.
These and other features will become better understood from the description that follows.
14a Date Recue/Date Received 2021-09-01 DETAILED DESCRIPTION
The composition and methods now will be described more fully hereinafter.
These embodiments are provided in sufficient written detail to describe and enable a person having ordinary skill in the art to make and use the claims, along with disclosure of the best mode .. for practicing the claims, as defined by the claims and equivalents thereof.
Likewise, modifications and other embodiments of the methods described herein will come to mind to one of ordinary skill in the art having the benefit of the teachings presented in the foregoing descriptions. Therefore, it is to be understood that the disclosure is not to be limited to the specific embodiments disclosed and that modifications and other embodiments .. are intended to be included within the scope of the appended claims.
Although specific terms are employed herein, they are used in a generic and descriptive sense only and not for purposes of limitation.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art. Although any methods and materials similar to or equivalent to those described herein can be used in the practice or testing of the claims, the exemplary methods and materials arc described herein.
Moreover, reference to an element by the indefinite article "a" or ''an" does not exclude the possibility that more than one element is present, unless the context clearly requires that there be one and only one element. The indefinite article "a" or "an" thus usually .. means "at least one."
The term "about" means within a statistically meaningful range of a value or values such as a stated concentration, length, molecular weight, pH, time frame, temperature, pressure or volume. Such a value or range can be within an order of magnitude, typically within 20%, more typically within 10%, and even more typically within 5% of a given value or range. The allowable variation encompassed by "about" will depend upon the particular system under study.
Abbreviations "Ph," "Pr" and "Bu" refer to phenyl, propyl and butyl, respectively.
Date Recue/Date Received 2020-07-24 The terms "substituent", "radical", "group", "moiety" and "fragment" may be used interchangeably.
The number of carbon atoms in a substituent can be indicated by the prefix "CAB"
where A is the minimum and B is the maximum number of carbon atoms in the substituent.
The term "alkyl" embraces a linear or branched acyclic alkyl radical containing from 1 to about 15 carbon atoms. In some embodiments, alkyl is a Ci_io alkyl, C1_6 _ Alkyl C13 alkyl radical. Examples of alkyl include, but are not limited to, methyl, ethyl, propyl, isopropyl, butyl, butyl, isobutyl, tert-butyl, sec-butyl, pentan-3-y1 (i.e., ¨
) and the like.
The term "alkenyl" refers to an unsaturated, acyclic hydrocarbon radical with at least one double bond. Such alkenyl radicals contain from 2 to about 15 carbon atoms. Non-limiting examples of alkenyl include ethenyl (vinyl), propenyl and butenyl.
The term "alkynyl" refers to an unsaturated, acyclic hydrocarbon radical with at least one triple bond. Such alkynyl radicals contain from 2 to about 15 carbon atoms. Non-limiting examples of alkynyl include ethynyl, propynyl and propargyl.
The verb forms of "comprise," "have" and "include," have the same meaning as used herein. Likewise, the verb forms of "describe", "disclose" and "provide" have the same meaning as used herein.
The term "aryl" refers to any monocyclic, bicyclic or tricyclic cyclized carbon radical, wherein at least one ring is aromatic. An aromatic radical may be fused to a non-aromatic cycloalkyl or heterocyclyl radical. Examples of aryl include phenyl and naphthyl.
The term "arylene" refers to a bivalent radical (as phenylene) derived from an aromatic hydrocarbon by removal of a hydrogen atom from each of two carbon atoms of the nucleus.
The term "transition metal," comprising the plural form thereof, refers to any element of d-block of the periodic table. Exemplary elements of a transition metal include those having atomic numbers 21 through 30, 39 through 48, 71 through 80, and 103-112.

Date Recue/Date Received 2020-07-24 The term "metal oxide" refers to a compound having a metal-oxygen bond, wherein oxygen has an oxidation number of -2. Exemplary metal oxides include sodium oxide, magnesium oxide, calcium oxide, aluminum oxide, lithium oxide, silver oxide, iron (II) oxide.
iron (III) oxide, chromium (VI) oxide, titanium (IV) oxide, copper (I) oxide, copper (II) oxide, zinc oxide, and zirconium oxide.
The term "inorganic oxide" refers to a compound formed between a non-carbon element and oxygen. Exemplary inorganic oxides include metal oxides, silicone oxide, phosphate oxide, and borate oxide, among others.
The term "silica" refers to a compound consisting essentially of silicon dioxide and includes the formula SiO2, The tetra "silicate" refers to a compound that includes an anionic silicon compound.
Exemplary silicates include ethyl silicate, methyl silicate, isopropyl silicate and butyl silicate, among others.
The term "silsesquioxane" refers to an organosilicon compound with the empirical chemical formula RSi0.3/2 where Si is the element silicon, 0 is oxygen and R
is, for example, hydrogen, alkyl, alkene, aryl, or arylene group. The term "silsesquioxane"
includes cage structures in which the units form a cage of n units in a designated T,, cage;
partially caged structures, in which the aforementioned cages are formed but lack complete connection of all units in the cage; ladder structures in which two long chains composed of RSiO3/2 units are connected at regular intervals by Si-0-Si bonds; and random structures which include RSiO3/2 unit connections without any organized structure formation.
The term "partially caged silsesquioxane" denotes a radical having the general formula:
Si ______________________________________ 0 R
0/ I OH) \ 0 /R 0 Si¨01¨SL

Si-0--Si Date Recue/Date Received 2020-07-24 The terms "compound," "resin compound," and "modified silicone resin" are used interchangeably and have the same meaning when referring to Formulas (I) and (II).
The phrase "neat formulation" refers to a formulation consisting of a defined composition of specified components, wherein the total amount of the specified components of the defined composition sums to 100 weight-percent. A person of ordinary skill in the art will recognize that not all formulations are "neat formulations," as a formulation can comprise a defined composition of specified components, wherein the total amount of the specified components of the defined composition sums to less than 100 weight-percent and a remainder of the formulation comprises other components, wherein the total amount of the specified components of the defined composition and the remainder sums to 100 weight-percent. The clastomer formulations disclosed herein sum to 100 weight-percent of the total amount of specified components and other components.
The chemical structures described herein are named according to IUPAC
nomenclature rules and include art-accepted common names and abbreviations where appropriate. The IUPAC nomenclature can be derived with chemical structure drawing software programs, such as ChemDraw (PerkinElmer, Inc.), ChemDoodle (iChemLabs, LLC) and Marvin (ChemAxon Ltd.). The chemical structure controls in the disclosure to the extent that an IUPAC name is misnamed or otherwise conflicts with the chemical structure disclosed herein.
Modified silicon resins New modified silicone resins and methods for their preparation and application are disclosed that provide unexpectedly superior thermal resistance and long-life operating characteristics as elastomers at high temperatures (e.g., 316 C). The resins incorporate benzene, phosphorous or other species into silicone backbones or side chains and produce modified silicone resins. The resins can be used to prepare elastomer formulations having improved theimal resistance for high temperature (for example, greater than 316 C) applications.
As detailed below, the new modified silicone resins may offer advantages over prior art silicone-based polymers used in high-temperature elastomeric resin applications. First, the Date Recue/Date Received 2020-07-24 resins may have demonstrable improved thermal performance. Second, tunable resins can be produced with controlled and desired molecular weights or viscosities, thereby enabling their use in formulations with other components. Third, a,co-hydroxyl-terminated groups can be generated as the terminal groups of siloxane resins so that they can be readily polymerized by common curing technologies (e.g., condensation curing using dibutyltin dilaurate, dibutltin octoate, etc). Fourth, different reactions with diverse structural choices can be used to produce various types of silicone modifications and material formulations.
Fifth, the disclosed resins remove thermally weak fragments, demonstrating the unexpectedly superior robust mechanical and thermal properties. These and other features of the new modified silicone resins and the methods directed thereto are more fully described below.
In a first aspect, a modified silicone resin of Foimula (I) is described:

HO¨Si ((0 P)(0 Si)n) OH
Mn R2 0 R2 (I) wherein RI, R2, and R3 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl;
n ranges from 1 to 10;
m ranges from 1 to 200; and p ranges from 2 to 1,000.
In some aspects, a modified silicone resin of Foimula (I) includes narrower ranges for n, m and p than provided above, wherein n ranges from 1 to 3; m ranges from 1 to 100; and p ranges from 10 to 500.
In certain aspects, a modified silicone resin of Formula (I) is described, wherein RI, R2, and R3 each being independently selected from a group consisting of H, Ci_g alkyl, C2.8 alkenyl, C2.8 alkynyl, and aryl. In certain aspects, a modified silicone resin of Formula (I) wherein RI, R2, and R3 each being independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl. propylenyl, butylenyl, acetylenyl, diacetylenyl, and aryl. In Date Recue/Date Received 2020-07-24 certain aspects, a modified silicone resin of Formula (I) specify RI, R2, and R3 each being independently selected from a group consisting of methyl and phenyl. In each of the foregoing aspects, the modified silicone resin include narrow ranges for n, m and p, wherein n ranges from 1 to 3; m ranges from 1 to 100; and p ranges from 10 to 500.
In one aspect, a modified silicone resin of Formula (I) is provided, wherein values for n, m and p to provide a compound of Formula (I) having a viscosity ranging from about 500 cSt to about 10,000 eSt.
In one aspect, a modified silicone resin of Formula (I) is provided, wherein a ratio of n to m ranges from about 1:1 to about 1:200.
In another aspect, a modified silicone resin of Formula (I) is provided, wherein n ranges from 1 to 5; m ranges from 1 to 100; and p ranges from 2 to 500. In another aspect, a modified silicone resin of Formula (I) is provided, wherein n ranges from 1 to

3; m ranges from 5 to 10; and p ranges from 2 to 100. In another aspect, a modified silicone resin of Formula (I) is provided, wherein n ranges from 1 to 10; m ranges from 5 to 100; and p ranges from 10 to 500.
Examples of modified silicone resins of Formula (I) are listed in Table I;
wherein values for n, m, and p are as described above.
Table I. Exemplary Resins of Formula (I) (i) HO Si ((0 __________________________________ P) (0 Si) OH
n rrlp (ii) HO Si ((0 P) (0 Si) \ OH
0 n n-fp Date Recue/Date Received 2020-07-24 HO¨Si ((0¨P) (\O¨Si)) OH
I n (iv) õ
HO¨Si¨O¨P) (0¨Si) OH
\\II n nri/p (V) HO¨Si ((0¨P) (0¨Si) OH
In m/p (vii) HO¨Si ((0¨P)(0¨Si)n) OH
n Date Re9ue/Date Received 2020-07-24 (viii) HO¨Si ((0¨P) (0¨Si)n) OH
In P

In another aspect, a modified silicone resin of Formula (II) having one of compositions (a)-(c) is described:
(a) a composition of Formula (II) comprising at least one of each of the following subunits:
( R8 Rio \
____________________________ 0 i X
R9 R"
A =

R13) Y; and ( di )z R7 ;
(b) a composition of Formula (II) comprising:

Date Recue/Date Received 2020-07-24 R6, 12 R6, 12 Rs Rio R6, 12 R6, 12 HO _________ Si (( 0 __ Si _______ 0¨Si X Si 0 Si) (0 Si) ) OH

111 y z R R7'13 R7' 13 R9 R7, 13 R7' 13 (II) or (c) a composition of Formula (II) made by a process comprising:

HO¨Si¨ X¨Si¨OH \Ii_N/ ( Si ¨O __ H
/ 1 \
contacting R9 R13 , and R7 in presence of an organic solvent;
wherein R6, R7, R8, R9, R1 , ¨
K R12 and R13 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl; X is selected from a group consisting of arylene, transition metal, inorganic oxide, and silsesquioxane; and t ranges from 1 to 10; y ranges from 1 to 200; and z ranges from 1 to 1,000 for compositions (a) or (b) of Formula (II).
In another aspect, a modified silicone resin of Formula (II) is described, wherein R6, R7, R8, R9, Rlo, R11, Rt2, and R'3 are each independently selected from a group consisting of H, C1_8 alkyl, C2-8 alkenyl, C2-8 alkynyl, and aryl. In another aspect, a modified silicone resin of Fotmula (II) is described, wherein R6, R7, R8, R9, R10, R11, K-12 and R13 are each independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl and aryl. In another aspect, a modified silicone resin of Formula (II) is described, wherein R6, R7, R8, R9, K-10, and R" are each independently selected from a group consisting of methyl and phenyl; and R12 and R13 are each independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl, and aryl.

Date Recue/Date Received 2020-07-24 In another aspect, a modified silicone resin of Formula (II) is described, wherein t ranges from 1 to 3; y ranges from 5 to 10; and z ranges from Ito 100.
In another aspect, a modified silicone resin of Formula (II) is described, wherein ratio oft to y ranges from about 1:1 to about 1:200.
Exemplary substituents X of Formula (II) for arylenes, transition metals, inorganic oxides, and silsesquioxanes are illustrated below in Table II.

Date Recue/Date Received 2020-07-24 Di gi X Table II. Exemplary substituents X of Formula (II).
cr) K, c R2 co R26 _ R28_ R3 R39 I/
Dl gi AlI --C)- i __ 0 i 0 i¨ Si¨O¨Si x o1 o1 R4 n /0" 1 0/1 CD 0/ \O
\ v 444 0 CD
Si ________ 01¨Sr I

1 1 R43-Si-1-0¨Si CD
Q. ___________________________________________________________________ 0 Si __ 0 Si 0 0 0/ 0 0/ 2 r..) c) R27 -N.) 5 ,SI-0¨SI
0 \R" -,1 R21 R22 U = 1 - 1 000 ¨C) \/,t.
______________________________________________ 0/i \O
R45 Ra6 R32 )z?
\Si/
\
o'r" \ 0 Q/
0H\

R33 ,0. 1 }31-1 )õ 0_SI i 1,0 R23 R24 \ 7 0 7 R3,0 \ 7 si_o_rsi 1 , --0--Zr I
R3fSi40 ¨Si ¨( )---( )-- __________________________________ 0/ \O 1/ 1/
Si-0¨Si \

IR3 o _______________________________________________________________________________ ____________________ Si _______________________________________________________________________________ _________________ n..---S1 [1 R55 \Sr _______________________________________________ /3 \
___________________________________________ \ / \
0 0 5 1 __ 0/
\O R5i1 >

Accordingly, exemplary modified silicone resins of Formula (II) are listed in Table Table III. Exemplary Modified Silicone Resins of Formula (II).
Resin X R6-134 ___ le R" R56 (1) CH3 R55-56 = CH3 Si \O

(2) \Si/ CH3 R55-56 = Phenyl (3( \o (3) R8-111 = CH3

(4) R6,7,12,13 CH3, Vinyl R8-11 = CH3

(5) R6,7,12,13 = CH3, Vinyl, Phenyl R23 Rza (9) /
Zr CI I3 R233 R24 opr \O

(10)Ti CH3 R21, R22 = 0Bu (11) CH3 R25 = Phenyl \O

Date Recue/Date Received 2020-07-24 Resin X R6 -13a ____ R4 R"
\
Si-0 , /

(12) Si¨OrSi CH3 R32-38 = CH3 R"-Si I 0¨Si,, 0 C( 0 /0" R36 / /
Si-0 Si \

\
Si-0 R33 /cc /R 3HA
\ (13) Si¨O-rSi 80 CH3 R32-38 = Phenyl R37-si4o¨Si, o I / I /
Si¨o¨Si IR4 , \Si/
(14) 0,---0 CH3 R45-48 = CH3 ___________________ 0.--_, 1 Si Si--/ 0 \

---- =

I R"
R53 0¨sr.
\ / \
(15) ¨0---"Sii 0 CH3 R49-54 = CH3 0\ /SI
\
R511-' R54 a Where more than one substituent is identified in Table III for R6-13 (that is, for Resins #4 and #5), each of R613 may be independently selected from those substituents.
Modified silicone resins of Formula (I) and/or Folinula (II) can be characterized for their molecular structure/composition by UV-Visible spectroscopy (UV-Vis), Infrared spectroscopy (IR), nuclear magnetic resonance spectroscopy (NMR), and elemental analysis;

Date Recue/Date Received 2020-07-24 for their molecular weight by gel permeation chromatography (GPC), and for their viscosity by viscometer or rheometer.
A modified silicone resin, as used herein, denotes a resin where at least one member of the resin backbone or side chains is replaced with a phosphorous group (as in Formula (I)) or an "X" moiety (as in Formula (II)). Without the claimed subject matter being bound by any particular theory, these structural units are expected to disrupt the degradation mechanism of siloxane materials at high temperatures.
Elastomer Formulations Comprising Modified Silicon Resin(s) In another aspect, an elastomer formulation comprises at least one modified silicone resin of Formula (I):
R1 R3 Ri HO Si ((0 __ P \( ______ OH Si)n) R2 0 R2 (I) wherein RI, R2, and R3 are each independently selected from a group consisting of H, alkyl.
alkenyl, alkynyl, and aryl;
n ranges from 1 to 10;
m ranges from 1 to 200; and p ranges from 2 to 1,000:
optionally, at least one silicate;
optionally, at least one silica;
at least one metal oxide; and at least one curing agent.
In one aspect of an elastomer formulation comprising at least one modified silicone resin of Formula (I), m ranges from 1 to 100; and p ranges from 10 to 500.
In one aspect of an elastomer formulation comprising at least one modified silicone resin of Formula (I), R1, R2, and R3 are each independently selected from a group consisting of Date Recue/Date Received 2020-07-24 IT, C1_8 alkyl, C2-8 alkenyl, C2-8 alkynyl, and aryl. In one aspect of an elastomer formulation comprising at least one modified silicone resin of Formula (I), RI, R2, and R3 are each independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl, and aryl. In one aspect of an elastomer formulation comprising at least one modified silicone resin of Formula (I), RI, R2, and R3 are each independently selected from a group consisting of methyl and phenyl. In these foregoing aspects, m ranges from 1 to 100; and p ranges from 10 to 500.
In one aspect of an elastomer formulation comprising at least one modified silicone resin of Formula (I), wherein n ranges from 1 to 10, m ranges from 1 to 100, and p ranges from 10 to 500, the at least one modified silicone resin comprises at least one of the species selected from Table I.
In one aspect of an elastomer formulation comprising at least one modified silicone resin of Formula (I), the at least one metal oxide comprises at least one of iron oxide (for example, FeO, Fe2O3 and Fe304), titanium oxide (for example, h02), cerium oxide (for example, Ce02), zinc oxide (for example, Zn0), and zirconium oxide (for example, ZrO2). In one aspect, the at least one metal oxide comprises at least one of iron oxide (for example, FeO, Fe2O3 and Fe304), and titanium oxide (for example, TiO2).
In one aspect of an elastomer formulation comprising at least one modified silicone resin of Formula (I), values for n, m and p provide a compound of Formula (I) having a viscosity ranging from about 500 cSt to about 10,000 cSt.
In one aspect of an elastomer formulation comprising at least one modified silicone resin of Formula (I), a ratio of n to m ranges from about 1:1 to about 1:200.
In one aspect of an elastomer formulation comprising at least one modified silicone resin of Formula (I), the at least one modified silicone resin of Formula (I) is present in an amount ranging from about 5 weight-percent to about 95 weight-percent; the at least one metal oxide is present in an amount ranging from about 2 weight-percent to about 80 weight-percent;
and the at least one curing agent is present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.

Date Recue/Date Received 2020-07-24 In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) is provided, wherein n ranges from 1 to 5, m ranges from 1 to 100, and p ranges from 2 to 500. In another aspect, the clastomer formulation comprises a modified silicone resin of Formula (I), wherein n ranges from 1 to 3; m ranges from 5 to 10; and p ranges from 10 to 500.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) is provided, wherein the at least one metal oxide can have a particle diameter size ranging from, for example, about 1 nanometer to about 5 micrometers, from about 25 nanometers to about 2 micrometers, and/or from about 50 nanometers to about nanometers.
In another aspect, an elastomer formulation comprising a modified silicone resin of Foiniula (I) is provided, wherein the at least one silicate is at least one of ethyl silicate, methyl silicate, isopropyl silicate, or butyl silicate.
In another aspect, an elastomer foimulation comprising a modified silicone resin of Formula (I) is provided, wherein the at least one silica can be fumed silica, functionalized silica, among others.
In another aspect, an elastomer foimulation comprising a modified silicone resin of Formula (I) is provided, wherein the modified silicone resin is selected from Table I.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) is provided, wherein values for n, m and p provide a compound of Formula (I) comprising a viscosity ranging from about 500 eSt to about 10,000 cSt.
In another aspect, the elastomer formulation comprises a modified silicone resin of Formula (1), wherein ratio of n to m ranges from about 1:1 to about 1:200.
In another aspect, elastomer formulations comprising the following compositions are .. provided: (a) the compound of Formula (I) present in an amount ranging from about 5 weight-percent to about 95 weight-percent; (b) at least one metal oxide present in an amount ranging from about 2 weight-percent to about 80 weight-percent; (c) optionally at least one silicate present in an amount ranging from about 0 weight-percent to about 25 weight-percent; (d) optionally at least one silica present in an amount ranging from about 0 weight-percent to ";CI
Date Recue/Date Received 2020-07-24 about 20 weight-percent; (e) at least one curing agent present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.
In another aspect, an elastomer formulation comprising at least one modified silicone resin of Formula (II) haying one of compositions (a)-(c) is described:
(a) a composition of Formula (II) comprising at least one of each of the following subunits:

( Rio \
I I
0 Si X Si 0 ____________________________________ R9 Rii i / I
Si \ I
\ R13 Y; and fsi i 0 )z I
R7 =
, (b) a composition of Formula (II) comprising:
Re, 12 R6, 12 R8 R10 R,12 R6, 12 HO Si ((0 Si 0 Si X Si 0 Si) (0 Si) ) OH
I I I I 1 t 1 y z R7, 13 R7' 13 R9 R-1-1 R7' 13 R7' 13 (II) , or (c) a composition of Formula (II) made by a process comprising:

Date Recue/Date Received 2020-07-24 R8 Rlo HO __________________ Si __ X Si OH \N41_N/ ( Si contacting i j11 , and in presence of an organic solvent;
wherein R6, R7, R8, R9, R1 , Rn, K-12 and R13 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl; X is selected from a group consisting of arylene, transition metal, inorganic oxide, and silsesquioxane; and t ranges from 1 to 10; y ranges from 1 to 200; and z ranges from 1 to 1,000 for compositions (a) or (b) of Formula (II);
optionally, at least one silicate;
optionally, at least one silica;
at least one metal oxide; and at least one curing agent.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is provided, wherein R6, R7, R8, R9, Rui, Rii, Ru, and K-13 are each independently selected from a group consisting of H, Ci_g alkyl, C2_8alkenyl, C2_8alkynyl, and aryl. In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is provided, wherein R6, R7, Rs, R9, Rio, RH, Ri2 and K-13 are each independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl.
diacetylenyl and aryl. In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is provided, wherein R6, R7, Rs, R9, RN, and Rll are each independently selected from a group consisting of methyl and phenyl; and R12 and R13 are each independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl, and aryl.
In another aspect, an elastomer formulation comprising a modified silicone resin of Foimula (II) is provided, wherein t ranges from 1 to 5; y ranges from 1 to 100; and z ranges Date Recue/Date Received 2020-07-24 from 1 to 1000. In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is provided, wherein t ranges from 1 to 3; y ranges from 5 to 100; and z ranges from 10 to 500.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is provided, wherein the at least one metal oxide can be selected from, for example, at least one of iron oxide (for example, FeO, Fe2O3 and Fe304), titanium oxide (for example, TiO2), cerium oxide (for example, Ce02), zinc oxide (for example, Zn0), and zirconium oxide (for example, ZrO2). In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is provided, wherein the at least one metal oxide is selected from at least one of iron oxide (for example, FeO, Fe2O3 and Fe304), and titanium oxide (for example, TiO2).
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is provided, wherein the at least one metal oxide can have a particle diameter size ranging from, for example, about 1 nanometer to about 5 micrometers, from about 25 nanometers Lo about 2 micrometers, and/or from about 50 nanometers to about nanometers.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is provided, wherein the optional at least one silicate is at least one of ethyl silicate, methyl silicate, isopropyl silicate, or butyl silicate.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is provided, wherein the optional at least one silica can be fumed silica, functionalized silica, among others.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is provided, wherein the modified silicone resin is selected from Table III.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is provided, wherein values for t, y and z provide a compound of Formula (II) comprising a viscosity ranging from about 500 cSt to about 10,000 cSt.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is provided, wherein ratio of n to m ranges from about 1:1 to about 1:200.

Date Recue/Date Received 2020-07-24 In another aspect, elastomer formulations comprising the following compositions are provided: (a) a modified silicone resin of Formula (II) present in an amount ranging from about 5 weight-percent to about 95 weight-percent; (b) at least one metal oxide present in an amount ranging from about 2 weight-percent to about 80 weight-percent; (c) optionally at least one silicate present in an amount ranging from about 0 weight-percent to about 25 weight-percent; (d) optionally at least one silica present in an amount ranging from about 0 weight-percent to about 20 weight-percent; (e) at least one curing agent present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.
In another aspect, an elastomer formulation comprising a modified silicone resin of Folinula (II) is selected from Formulations #109, #110, and ##116-124:
Formulation # Starting Resin2 Starting Resin2 Iron oxide3 Curinf (% w/w) (% w/w) (% w/w) agent (% w/w) 109 I 501 (Resin (2)) 45 5 (b) 110 59 (Resin (2)) 36 5 (b) 116 24.7 (Resin (1)) 24.7 (Resin (1)) 43 (TiO2) 7.6 (c) 117 25.5 (Resin (1)) 25.5 (Resin (1)) 43 6 (c) 118 49.5 (Resin (1)) 42.5 0.5 (a), 7.5(c) 119 62.95 (Resin (1)) 34.55 2.5 (c) 120 73.5 (Resin (1)) 25 1.5 (b) 121 32.25 (Resin (1)) 32.25 (Resin (1)) 33 2.5 (b) 122 32 (Resin (1)) 32 (Resin (1)) 33 (TiO2) 3 (b) 123 29 (Resin (1)) 29 (Resin (1)) 27, 12 (TiO2) 3 (c) 124 61 (Resin (2)) 24, 12 (h02) 3 (b) -Numerical values represent weight-percent contribution of component to elastomer formulation.
2Starting resin(s) correspond to those resins having the structure presented in Table III.
3Iron oxide at the weight-percent contribution in the elastomer formulation is presented. When TiO2 replaces the iron oxide in the clastomer formulation, then only the weight-percent contribution of TiO2 is presented (e.g., Formulations 116 and 122). When TiO2 supplements the iron oxide in the elastomer formulation, then the first weight-percent contribution reflects that of iron oxide and the second weight-percent contribution reflects that of TiO2 (e.g., Formulations 123 and 124).
4Curing agents: a ¨ dibutyltin dilaurate; b ¨ tris(dimethylamino)methylsilane;
c-ethyltriacetoxysilane Date Recue/Date Received 2020-07-24 In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is described, further comprising at least one silicate. The at least one silicate comprises at least one of ethyl silicate, methyl silicate, isopropyl silicate and butyl silicate. In these aspects, R6, R7, R8, R9, Rio, Rit, K-12, and R13 of Formula (II) are each independently selected from a first group consisting of H, alkyl, alkenyl, alkynyl, and aryl; a second group consisting of H, C1_8 alkyl, C2_8 alkenyl, C2-8 alkynyl, and aryl; a third group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl and aryl; and a fourth group consisting methyl and phenyl. In these aspects, an elastomer formulation comprising a modified silicone resin of Formula (II) and at least one silicate is .. provided, wherein R6, R7, R8, R9, R19, and R11 are each independently selected from a group consisting of methyl and phenyl; and R12 and R13 are each independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl, and aryl.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) having R6, R7, R8, R9, RH, K-11, R12, and R13 each being independently selected from a group consisting of methyl and phenyl and further comprising at least one silicate are provided, wherein the at least one modified silicone resin of Formula (II) is present in an amount ranging from about 5 weight-percent to about 95 weight-percent; the at least one metal oxide is present in an amount ranging from about 2 weight-percent to about 80 weight-percent;
the at least one silicate is present in an amount ranging from 0 weight-percent to about 25 weight-percent; the at least one silica present in an amount ranging from about 0 weight-percent to about 20 weight-percent; and the at least one curing agent is present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is selected from Foimulations #102, 4106, #107, ##112-114, #125 and #126:
Date Recue/Date Received 2020-07-24 Formulation # Starting Resin2 Iron oxide3 Ethyl Curing (')/0 w/w) ( /0 w/w) silicate4 agent5 (/o VV/W) (% w/w) 102 52 (Resin (2)) 45 2.5 0.5 106 49.5 (Resin (2)) 45 5 0.5 107 50.5 (Resin (2)) 45 4 0.5 112 52.5 (Resin (1)) 45 2 0.5 113 49.5 (Resin (1)) 45 5 0.5 114 52 (Resin (1)) 45 2.5 0.5 125 58.5 (Resin (2)) 36 (1102) 5 0.5 126 58.5 (Resin (2)) 24, 12 (h02) 5 0.5 1Numerical values represent weight-percent contribution of component to elastomer formulation.
2Starting resin(s) correspond to those resins having the structure presented in TableIII.
3Iron oxide at the weight-percent contribution in the elastomer formulation is presented. When TiO2 replaces the iron oxide in the elastomer formulation, then only the weight-percent contribution of TiO2 is presented (e.g., Formulation 125). When TiO2 supplements the iron oxide in the elastomer formulation, then the first weight-percent contribution reflects that of iron oxide and the second weight-percent contribution reflects that of TiO2 (e.g., Formulation 126).
4Ethyl silicate at the weight-percent contribution in the elastomer formulation is presented.
5Dibutyltin dilaurate In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is described, further comprising at least one silica. In some aspects, the at least one silica comprises at least one of fumed silica and functionalized silica.
In these aspects, R6, R7, Rs, R9, RI , R11, ¨12, and R13 of Formula (II) are each independently selected from a first group consisting of H, alkyl, alkenyl, alkynyl, and aryl; a second group consisting of H, Ci_s alkyl, C2_8 alkenyl, C2_8 alkynyl, and aryl; a third group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl and aryl;
and a fourth group consisting methyl and phenyl. In these aspects, an elastomer fonnulation comprising a modified silicone resin of Formula (II) and at least one silicate is provided, wherein R6, R7, R8, R9, RN, and R11 are each independently selected from a group consisting of methyl and phenyl; and R12 and 1113 arc each independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl, and aryl.

Date Recue/Date Received 2020-07-24 In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) having R6, R7, R8, R9, Rto, R11, K-12, and R13 each being independently selected from a group consisting of methyl and phenyl, and further comprising at least one silica selected from least one of fumed silica and functionalized silica is provided, wherein the at least one modified silicone resin of Formula (II) is present in an amount ranging from about 5 weight-percent to about 95 weight-percent; the at least one metal oxide is present in an amount ranging from about 2 weight-percent to about 80 weight-percent; the at least one silica is present in an amount ranging from 0 weight-percent to about 20 weight-percent;
and the at least one curing agent is present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is described, wherein R6, R7, R8, R9, RA, Rt2, and R13 arc each independently selected from a group consisting of methyl and phenyl, and wherein the elastomer formulation further comprises at least one silicate and at least one silica.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is described, wherein R6, R7, R8, R9, Rio, RII, R12, and R13 are each independently selected from a group consisting of methyl and phenyl, and further comprising at least one silicate and at least one silica, wherein the at least one silicate comprises at least one of ethyl silicate, methyl silicate, isopropyl silicate and butyl silicate and the at least one silica comprises at least one of fumed silica and functionalized silica.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (II) is described, wherein R6, R7, R8, R9, RH), R11, R12, and R13 are each independently selected from a group consisting of methyl and phenyl, and further comprising at least one silicate comprising at least one of ethyl silicate, methyl silicate, isopropyl silicate and butyl silicate and at least one silica comprising at least one of fumed silica and functionalized silica, wherein the at least one modified silicone resin of Formula (II) is present in an amount ranging from about 5 weight-percent to about 95 weight-percent;
the at least one metal oxide is present in an amount ranging from about 2 weight-percent to about 80 weight-percent; the at least one silicate is present in an amount ranging from 0 weight-percent to about 25 weight-percent; the at least one silica is present in an amount ranging from 0 weight-Date Recue/Date Received 2020-07-24 percent to about 20 weight-percent; and the at least one curing agent is present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.
In another aspect, an elastomer formulation comprises at least one modified silicone resin of Formula (I):

I I I
HO¨Si ((0 P) ( 0 Si)m) OH
1 11 n 1 P
R2 0 R2 (I) and at least one modified silicone resin of Foimula (II) having one of compositions (a)-(c):
(a) a composition of Folmula (II) comprising at least one of each of the following subunits:
( R8 _____________________________ 0 si x si 0 _____ It;

(d1 \
I
IV/
Y ; and ( di o )z I
R7 =
, (b) a composition of Formula (I1) comprising:

Date Recue/Date Received 2020-07-24 R6, 12 R6, 12 Rs R10 R6, 12 R6, 12 HO¨Si (( 0¨Si-0 Si X Si 0 Si) (0 Si) ) OH
z R7' 13 713 R9 R11 R7' 13 R7' 13 (II) or (c) a composition of Formula (II) made by a process comprising:

HO __________________ Si __ X __ Si ____________ OH \N_sli_N/ __ ( Si ¨O H
/ 13 1 1 \ 1 contacting , and in presence of an organic solvent;
wherein RI, R2, R3, R6, ¨ 7, K R8, R9, RN, R11, R12 and R13 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl; X is selected from a group consisting of arylene, transition metal, inorganic oxide, and silsesquioxane; and t ranges from 1 to 10; y ranges from 1 to 200; and z ranges from 1 to 1,000 for compositions (a) or (b) of Formula (II).
optionally, at least one silicate;
optionally, at least one silica;
at least one metal oxide; and at least one curing agent.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (II) is provided, wherein 1(1, R2, R3, R6, R7, R8, R9, R10, R11, R12 and R13 are each independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl and aryl.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (II) is provided, wherein RI, R2, R3, R6, R7, Rs, R9, R10, and R11 arc each independently selected from a group consisting of methyl and phenyl; and R12 and R13 Date Recue/Date Received 2020-07-24 are each independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl, and aryl.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (II) is provided, wherein n ranges from 1 to 5; m ranges from 1 to 200; p ranges from 2 to 1000; and wherein t ranges from 1 to 5; y ranges from 1 to 200; and z ranges from 2 to 1000. In another aspect, an elastomer formulation comprising a modified silicone resin of Foimula (I) and Formula (II) is provided, wherein n ranges from 1 to 3; m ranges from 1 to 100; and p ranges from 10 to 500; and wherein t ranges from 1 to 3; y ranges from 1 to 100; and z ranges from 10 to 500. In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (II) is provided, wherein n ranges from 1 to 3, m ranges from 5 to 100; and p ranges from 10 to 300, and wherein t ranges from 1 to 3; y ranges from 5 to 100; and z ranges from 10 to 300.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (II) is provided, wherein R1, R2, and R3 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl and wherein R. R1, le, R9, Rm, Rii, K-12, and R13 are each independently selected from a group consisting of It, C1_8 alkyl, C2_8 alkenyl, C2_8 alkynyl, and aryl. In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (II) is provided, wherein R1, R2, and R3 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl and wherein R6, R7, Rs, R9, Rio, R'2, and R13 are each independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl.
butylenyl, acetylenyl, diacetylenyl, and aryl. In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Fonnula (II) is provided, wherein R1, R2, and R3 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl and wherein R6, R7, R8, R9, R19, R11, R12, and R13 are each independently selected from a group consisting of methyl and phenyl.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (II) is provided, wherein R1, R2, R3, R6, R7, Rs, R9, Rio, Rit, Ri2, and R13 are each independently selected from a first group consisting of H, C1_8 alkyl, C2_8 alkenyl, C2-8 alkynyl, and aryl; a second group consisting of a third group consisting of methyl, ethyl, Date Recue/Date Received 2020-07-24 propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl and aryl; and a third group consisting methyl and phenyl. In those aspects where both Formula (I) and Formula (II) is provided, wherein RI, Rz, R3, R6, R7, R8, R9, R10, and R11 are each independently selected from a group consisting of methyl and phenyl, R12 and R13 of Foiinula (II) are each independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl, and aryl.
In another aspect, an elastomer fotmulation comprises a modified silicone resin of Formula (I) and Formula (II) is provided, wherein the at least one modified silicone resin of Faimula (I) is present in an amount ranging from about 5 weight-percent to about 95 weight-percent; the at least one metal oxide is present in an amount ranging from about 2 weight-percent to about 80 weight-percent; and the at least one curing agent is present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (II) is provided, wherein the elastomer formulation is Formulation #108 or #111:
Iron Curing Formula (I) Formula (II) Formulation # oxide agent (% w/w) ( /0 w/w) (0/0 w/w) % w/w) 108 6 [Resin (i)] 49.5 [Resin (#2)] 44 0.5 (a) 111 5 [Resin (i)] 47 [Resin (#2)] 44 4 (b) 1 Curing agents: a - dibutyltin dilaurate; b - tris(dimethylamino)methylsilane In another aspect, the Elastomer Foimulation #108 or #111 is provided, wherein the iron oxide comprises Fe2O3 having a particle size ranging from about 0.5 pm to about 5 pm, and the curing agent is at least one of dibutyltin dilaurate, tris(dimethylamino)methylsilane, and ethyltriacetoxysilane.
In another aspect, an elastomer fonnulation comprising a modified silicone resin of Follnula (I) and Formula (II) is described, further comprising at least one silicate. In some aspects, the at least one silicate comprises at least one of ethyl silicate, methyl silicate, isopropyl silicate and butyl silicate. In these aspects, R1, R2, R3 of Formula (I) and R6, R7, R8, R9, R10, R11, R'2, and R13 of Foimula (II) are each independently selected from a first group Date Recue/Date Received 2020-07-24 consisting of group consisting of H, alkyl, alkenyl, alkynyl, and aryl; a second group consisting of H, Ci_8 alkyl, C2-8 alkenyl, C2-8 alkynyl, and aryl; a third group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl and aryl; and a fourth group consisting methyl and phenyl. In these aspects, R1, R2, R3 of Formula (I) are as described above for each of the respective first, second, third and fourth groups, and R6, R7, R8, R9, R10, and I of Formula (II) are each independently selected from a group consisting of methyl and phenyl; and RI2 and R13 of Formula (II) are each independently selected from a group consisting of methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl, and aryl.
In another aspect, an elastomer fatinulation comprising a modified silicone resin of Formula (I) and Formula (II) is described, wherein le, R2, and R3 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl, wherein R6, R7, R8, R9, RI , R.11, R12, and R13 are each independently selected from a group consisting of methyl and phenyl and further comprising at least one silicate, wherein the at least one modified silicone resin of Formula (I) is present in an amount ranging from about 5 weight-percent to about 95 weight-percent; the at least one metal oxide is present in an amount ranging from about 2 weight-percent to about 80 weight-percent; the at least one silicate is present in an amount ranging from 0 weight-percent to about 25 weight-percent; the at least one silica present in an amount ranging from about 0 weight-percent to about 20 weight-percent; and the at least one curing agent is present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (II) is selected from Formulation #104 or #105:
Iron Ethyl Curing Formula (I) Formula (H) Formulation # oxide Silicate agent (0/0 w/w) (% w/w) 0/0 w/w) (0/0 w/w) (0/0 w/w) 104 8 [Resin (ii)] 45 [Resin (#2)] 44 2.5 0.5 , 105 7 [(Resin (i)] 46 [Resin (#2)] 44 2.5 0.5 1 Dibutyltin dilaurate In another aspect, Elastomer Formulation #104 or #105 is provided, wherein the iron oxide comprises Fe2O3 having a particle size ranging from about 0.5 p.m to about 5 p.m, and Date Recue/Date Received 2020-07-24 the curing agent is at least one of dibutyltin dilaurate, tris(dimethylamino)methylsilane; and ethyltriacetoxysilane, among others, as well as combinations thereof In another aspect, an elastomer formulation comprising a modified silicone resin of Foimula (I) and Formula (II) is described, wherein R1, R2, and R3 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl, wherein R6, R7, R8, R9, R' , R--, R12, and R13 are each independently selected from a group consisting of methyl and phenyl, wherein the elastomer formulation further comprises at least one silica. In some aspects, the at least one silica comprises at least one of fumed silica and functionalized silica.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Faimula (II) is described, wherein R1, R2, and R3 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl, wherein R6, R7, R8, R9, R", RH, R'2, and R13 are each independently selected from a group consisting of methyl and phenyl and further comprising at least one silica selected from least one of fumed silica and functionalized silica, wherein the at least one modified silicone resin of Folinula (I) is present in an amount ranging from about 5 weight-percent to about 95 weight-percent;
the at least one metal oxide is present in an amount ranging from about 2 weight-percent to about 80 weight-percent; the at least one silica is present in an amount ranging from 0 weight-percent to about weight-percent; and the at least one curing agent is present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.
20 In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (II) is described, wherein RI, R2, and R3 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl, wherein R6, R7, R8, R9, Rio, R11, K-12, and R13 are each independently selected from a group consisting of methyl and phenyl, wherein the elastomer Formulation further comprises at least one silicate and at least one silica.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (II) is described, wherein RI, R2, and R3 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl, wherein R6, R7, R8, R9, Rio, RH, K-12, and R13 are each independently selected from a group consisting of methyl and phenyl, and further comprising at least one silicate and at least one silica is provided, wherein Date Recue/Date Received 2020-07-24 the at least one silicate comprises at least one of ethyl silicate, methyl silicate, isopropyl silicate and butyl silicate and the at least one silica comprises at least one of fumed silica and functionalized silica.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (H) is described, wherein R1, R2, and R3 are each independently selected from a group consisting of H, alkyl, alkenyl, alkynyl, and aryl, wherein R6, R7, R8, R9, Rii, R12, and R13 are each independently selected from a group consisting of methyl and phenyl, and further comprising at least one silicate comprising at least one of ethyl silicate, methyl silicate, isopropyl silicate and butyl silicate and further comprising at least one silica comprising at least one of fumed silica and functionalized silica is provided, wherein the at least one modified silicone resin of Formula (I) is present in an amount ranging from about 5 weight-percent to about 95 weight-percent; the at least one metal oxide is present in an amount ranging from about 2 weight-percent to about 80 weight-percent; the at least one silicate is present in an amount ranging from 0 weight-percent to about 25 weight-percent;
the at least one silica is present in an amount ranging from 0 weight-percent to about 20 weight-percent;
and the at least one curing agent is present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.
In another aspect, Elastomer Formulation 17115 is described:
Iron Ethyl Curing Formula (I) Formula (II) Formulation # oxide Silicate agent (% w/w) (% w/w) (0/0 w/w) ( /0 w/w) CY0 w/w) 115 55.7 [Resin (i)] 6.55 [Resin (#2)] 27.11 1.96 (Ethyl 0.54 silicate);
8.14 (SiO2) Dibutyltin dilauratc In another aspect, Formulation #115 is provided, wherein the iron oxide comprises Fe2O3 having a particle size ranging from about 0.5 om to about 5 um, and the curing agent is at least one of dibutyltin dilaurate, tris(dimethylamino)methylsilane; and ethyltriacetoxysilane, among others, as well as combinations thereof.

Date Recue/Date Received 2020-07-24 In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (II) is provided, wherein the at least one metal oxide can be selected from, for example, at least one of iron oxide (for example, FeO, Fe2O3 and Fe304), titanium oxide (for example, TiO2), cerium oxide (for example, Ce02), zinc oxide (for example, Zn0), and zirconium oxide (for example, ZrO2). In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (II) is provided, wherein the at least one metal oxide is selected from at least one of iron oxide (for example, FeO, Fe2O3 and Fe304) and titanium oxide (for example, h02).
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (II) is provided, wherein the at least one metal oxide can have a particle diameter size ranging from, for example, about 1 nanometer to about 5 micrometers, from about 25 nanometers to about 2 micrometers, and/or from about 50 nanometers to about 500 nanometers.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Formula (II) is provided, wherein the at least one silicate is at least one of ethyl silicate, methyl silicate, isopropyl silicate, or butyl silicate.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (1) and Foimula (11) is provided, wherein the optional at least one silica can be fumed silica, functionalized silica, among others.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) and Foimula (II) is provided, wherein the exemplary modified silicone resins of Formula (I) are listed in Table I and wherein the exemplary modified silicone resins of Formula (II) are listed in Table III.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) in combination with a modified silicone resin of Formula (II) is provided, wherein values for n, m and p of Formula (I) provide an overall resin combination having a viscosity ranging from about 500 cSt to about 10,000 cSt. In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) in combination with a modified silicone resin of Formula (II) is provided, wherein values for t, y and z of Formula (II) provide an overall resin combination having a viscosity ranging from about 500 cSt to about 10,000 cSt.
Date Recue/Date Received 2020-07-24 In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) in combination with a modified silicone resin of Formula (II) is provided, wherein values for n, m and p of Formula (I) and wherein values for t, y and z of Formula (II), provide an overall resin combination having a viscosity ranging from about 500 cSt to about 10,000 cSt.
In another aspect, an elastomer formulation comprising a modified silicone resin of Formula (I) is provided, wherein ratio of n to m ranges from about 1:1 to about 1:200; in combination with a modified silicone resin of Formula (II), and wherein ratio oft to y ranges from about 1:1 to about 1:200.
In another aspect, elastomer formulations comprising the following compositions are disclosed: (a) a modified silicone resin of Formula (I) and Formula (II) (each independently) present in an amount ranging from about 5 weight-percent to about 95 weight-percent; (b) at least one metal oxide present in an amount ranging from about 2 weight-percent to about 80 weight-percent; (c) at least one silicate present in an amount ranging from about 0 weight-percent to about 25 weight-percent; (d) optionally at least one silica present in an amount ranging from about 0 weight-percent to about 20 weight-percent; and (e) at least one curing agent present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent, provided that the total amount of the components sums to 100 weight-percent for neat formul ati on s GENERAL SYNTHETIC SCHEMES
The compounds of the present disclosure can be prepared using the methods illustrated in the general synthetic schemes and experimental procedures detailed below. These general synthetic schemes and experimental procedures are presented for purposes of illustration and are not intended to be limiting. The starting materials used to prepare the compounds of the present disclosure are commercially available or can be prepared using routine methods known in the art. Representative procedures for the preparation of modified silicone resins of Formula (I) and Formula (II) are outlined below in Schemes I ¨III.

Date Recue/Date Received 2020-07-24 A modified silicone resin of Formula (I) is prepared with methyl/phenyl phosphonic acid or methyl/phenyl phosphonic dichloride. An exemplary direct coupling reaction is presented in Scheme I.
(B) , 1 ( Si H

Cl¨P--Cl ____________________ *- HO P)-(0 Si) )0H
IF I H m 0 R2 0 R2 r Here n = 1 (A) (C) (Scheme I) Structure (C) is an example of Formula (I). The ratios of the starting materials in Scheme I will affect the molecular weights and viscosities of the modified silicone resins as well as the thermal capability of the elastomers. The mole ratios of phosphorous units (A) to starting siloxane oligomeric unit (B) (that is, 1-0¨Si(R1)(R2)¨]), ranging from about 0.55 to about 1, can provide modified silicone resins (L) with viscosities ranging from about 500 cSt to about 10,000 cSt, as measured by a viscometer. Elastomer formulations displaying improved thermal resistance and maintaining superior mechanical properties can be prepared with modified silicone resins that include a mole ratio of phosphorous units (that is, [-0¨
P(0)(R3)¨] of resin (C)) to single siloxane oligomeric units (that is, 1-0¨Si(R1)(R2)¨] of resin (C))) ranging from about 1:4 to about 1:100.
In terms of Formula (I), the values for n, m and p can be adjusted to provide tunable resin compounds of Formula (I) with a viscosity ranging from about 500 cSt to about 10,000 cSt, as measured by a viscometer. Likewise, the ratio of n to m of resin compounds of Formula (I) ranges from about 1:1 to about 1:200.

Date Recue/Date Received 2020-07-24 A modified silicone resin of Formula (II) can be prepared in several different types of reactions. For example, 1,4-bis(hydroxydimethylsily0-benzene has two hydroxyl groups on silicone atoms that display different reactivity as compared to hydroxyl-terminated siloxanes.
Thus, a two-step process is used to include phenyl material into the silicone backbone and hydroxyl as the terminating groups as shown below in Schemes II and III.
(B) I

\ I /
N¨Si¨N
Rs Rio / 1,, =\ R12 Ra Rio R12 HO¨Si Si¨OH R1"
1 i R9 R11 R13 R9 R,, Ri, (A) (C) (Scheme II) (D) i R12 R8 __________ R10 R12 ki¨CI-H
R6 R12 R8 Rlo R12 Rs R13 Re __________ Rii Ri3 R7 R13 Rs R,, R,3 A i Here t = 1 (C) (E) (Scheme III) Date Recue/Date Received 2020-07-24 As shown in Scheme II, the first step is the amination of 1,4-bis(hydroxydimethylsily1)-benzene species (A) with bis(dimethylamino)dimethylsilane (B) to form the amidatcd phenyl species (C), which is usually performed in an organic solvent, such as toluene, at a temperature ranging from about 80 C to about 140 C. As shown in Scheme III, the second step is the direct coupling of siloxane oligomer (El) and the phenyl unit (c) with production of the modified silicone resin (E) and the release of dimethylamine (not shown). Schemes II and III can be perfoimed sequentially in the same reaction vessel under the same conditions (for example, in the same organic solvent).
Schemes I-III are typically perfotmed in an organic solvent. Common organic solvents used can be aprotic solvents comprising toluene, benzene, tetrahydrofuran (THF), acetonitrile, and N,N-dimethylformamide (DMF), among others.
Structure (E) in Scheme III is a species of Formula (II). The mole ratio of the two starting components of Scheme III (comprising the reaction conditions) determines the molecular weights and viscosities of the resultant modified silicone resins.
The ratios of the aminated phenyl species (C) to siloxane units in oligomer (D) can range from about 0.55 to about 1 in Scheme III to provide the resultant modified silicone resins (E) having viscosities ranging from about 500 cSt to about 10,000 cSt, as measured by a viscometer.
Because the hydroxyl-tenninated siloxane can be used in an excess amount, modified silicone resins will also be hydroxyl-terminated. Such hydroxyl groups are attached to siloxane and are readily polymerizable.
The mole ratio of phenyl units to single siloxane oligomeric units in modified silicone resin is an additional important consideration related to thermal resistant properties of the resultant elastomer formulations. The starting siloxane oligomers can contain various numbers of single siloxane units (for example, -Si(CH3)2-0-). The thermal resistant properties of the resultant modified silicone resins should be improved with increasing numbers of phenyl units present. However, elastomers containing such highly phenyl-substituted silicone resins can display compromised mechanical properties. Thus, elastomer formulations displaying improved thermal resistance and maintaining superior mechanical properties can be prepared with modified silicone resins that include a ratio of phenyl units to single siloxane units from about 1:5 to about 1:200.

Date Recue/Date Received 2020-07-24 In terms of Formula (II), the values for t, y and z can be adjusted to provide tunable resin compounds of Formula (II) with a viscosity ranging from about 500 cSt to about 10,000 cSt, as measured by a viscometer. Likewise, the ratio oft to y of resin compounds of Formula (II) ranges from about 1:1 to about 1:200.
For reactions that yield a modified silicone resin of Formula (I), bi-functional phosphorous groups can include, for example, methylphosphonic dichloride, phenylphosphonic dichloride, methyl diehlorophosphate, methylphosphonic acid, phenylphosphonic acid, and phenyl dichlorophosphate, among others.
For reactions that yield a modified silicone resin of Formula (II) having benzene groups, bifunctional benzene groups can include, for example, 1,4-bis(hydroxyldimethylsilyl)benzene, 1,3-bis(hydroxy-ldimethylsilypbenzene, 1,4-bis(dimethylsilyl)benzene, 1,3-bis(dimethylsily1) benzene, 1,4-dihalogenbenzene, and 1,3-dihalogen benzene.
For reactions that yield a modified silicone resin of Formula (1) or (II) having siloxane groups, bi-functional siloxanes can include, for example, co-dichlorosiloxanes or a,m-dihydroxylsiloxanes with molecular weights from about 400 to about 10,000.
Polymerization reaction resulting in production of the modified silicone resins is performed under an inert atmosphere condition. The reaction temperature for modified silicone resins can be from about room temperature to about 140 C. Reactions can be performed under neat conditions or with a suitable organic solvent. Suitable organic solvents used can be aprotic solvents comprising toluene, benzene, tetrahydrofuran (THF), acetonitrile, and N,N-dimethylformamide (DMF), among others.
The elastomer formulations comprising the foregoing various compositions can be thoroughly mixed manually or by a mixer equipment, degassed under vacuum, casted into a mold, and left at ambient condition. The elastomers can be cured from about 30 min to about 2 days.
Date Recue/Date Received 2020-07-24 EXAMPLES
The following examples are merely illustrative, and do not limit this disclosure in any way. Example 1 describes the preparation of a modified silicone. Examples 2 ¨
8 describe synthetic procedures for modified silicone resins (i), (ii), and (iv) of Formula (I) and modified silicone resins (3), (4), (5) of Formula (II). Example 9 describes procedure for preparing an elastomer formulation comprising modified silicone resin (2). Example 10 describes procedure for preparing an elastomer formulation comprising modified silicone resins (2) and (ii).
Modified Silicone Resins:
Example 1: Modified Silicone M101 To a solution of 1,4-bis(hydroxydimethylsilyl)benzene (2.575 g, Gelest) in toluene at 110 C was slowly added bis(dimethylamino)vinylmethylsilane (1.66 g, Gelest) under inert atmosphere within 2 h. The mixture was stirred at 110 C for 2 h and then solvent was evaporated, yielding the modified silicone material M101.
Example 2: Modified Silicone Resin (3) of Formula (II) To a solution of 1,4-bis(hydroxydimethylsilyl)benzene (5.0 g, Gelest) in toluene at 110 C was slowly added bis(dimethylamino)dimethylsilane (6.75 g. Gelest). The mixture was stirred at 110 C overnight and then the solvent was removed by vacuum.
Polydimethylsiloxane (16.2 g) (Mn 550, Gelest) was added to the mixture and stirred at 80 C
overnight, yielding a viscous modified silicone resin (3).
Example 3. Modified Silicone Resin (4) of Formula (II) To a solution of 1,4-bis(hydroxydimethylsilyl)benzene (2.055 g, Gelest) in toluene was added bis(dimethylamino)vinylmethylsilane (1.82 g, Gelest) under dinitrogen atmosphere. The mixture was stirred at 80 C for 10 min then raised to 110 C. A liquid of vinylmethylsiloxane-dimethylsiloxane copolymer (Mn ¨600, 3.151 g, Gelest) was then added and the mixture was stirred at 110 C for 22 h to produce the viscous resin (4).

Date Recue/Date Received 2020-07-24 Example 4. Modified Silicone Resin (5) of Formula (II) A mixture of 1,4-bis(hydroxydimethylsilyl)benzene (4.65 g, Gelest), 1,3-dichloro-L1,3,3-tetramethyldisiloxane (3.06 g, Gelest) and 1,7-dichloro-octamethyltetrasiloxane (5.41 g. Gelest) was mixed at room temperature for 1 h, 30 C lh, 50 C 1 h, and 110 C
63 h. To this solution was added silanol-terminated diphenylsiloxane-dimethylsiloxane copolymer (Mw 950, Gelest) and vinylmethylsiloxane-dimethylsiloxane copolymer (Mn ¨600, Gelest).
The mixture was stirred at 110 C for 24 h to yield viscous resin (5).
Example 5: Modified Silicone Resin (i) of Formula (I) A mixture of methylphosphonic acid (6.4 g, Aldrich) and polydimethylsiloxane (Mn 550, 48.7 g, Gelest) in toluene was stirred at 150 C for 24 h. Removal of toluene yielded viscous modified silicone resin (i).
Example 6: Modified Silicone Resin (ii) of Formula (I) Phenylphosphonic dichloride (7.0 g, Aldrich) was added into 26.3 g of polydimethylsiloxane (Mn 550, Gelest) and the mixture was stirred at room temperature under vacuum overnight. Mixture became viscous and was ready for elastomer formulations.
Example 7: Modified Silicone Resin (ii) of Formula (I) A mixture of phenylphosphonie acid (28.5 g, Aldrich) and polydimethylsiloxane (Mn 550,116.6 g, Gelest) was dissolved in toluene in a 500-mL round-bottom flask equipped with a stirrer, a Dean-Stark trap and a condenser. The flask was heated at 70 C for 15 h followed by heating at 110 C for 3 h. The mixture was then raised to 150 C to collect water (6.5 mL).
Toluene was removed by vacuum and the viscous modified silicone resin (ii) product was collected.
Example 8: Modified Silicone Resin (iv) of Formula (I) A mixture of methylphosphonic acid (2.0 g, Aldrich), 1,3-dichloro-1,1,3,3-tetramethyldisiloxane (2.57 g, Aldrich) and 1,7-dichloro-octamethylietrasiloxane (4.53 g, Aldrich) was stirred at 80 C for 24 hours. To this solution was added silanol-terminated diphenylsiloxane-dimethylsiloxane copolymer (4.6 mL, Gelest). The mixture was heated at 100 C for 68 h and produced a resin with viscosity at ¨1500cP.

Date Recue/Date Received 2020-07-24 Elastomer Formulations:
The elastomer formulations disclosed herein can include at least one modified silicone resin having the structure of Formulas (I) and/or (II), at least one type of metal oxide, optionally at least one silicate (e.g., ethyl silicate), optionally at least one silica, and at least one curing agent. The modified silicone resin(s) can represent from about 10 weight-percent to about 95 weight-percent of the elastomer formulation. The metal oxide of the elastomer formulation includes oxide particulates having a particle size (diameter) ranging from about 1 nanometer to about 5 micrometers. The elastomer formulations can include a metal oxide from about 2 weight-percent to about 80 weight-percent in the formulation.
Elastomer formulations may use iron oxide (for example, FeO, Fe2O3 and Fe304), titanium oxide (for example, TiO2), cerium oxide (for example, Ce02), zinc oxide (for example, Zn0), and zirconium oxide (for example, ZrO2), or a mixture of these oxides. Ethyl silicate can be present from about 0 weight-percent to about 25 weight-percent in the elastomer formulations.
Silica can be present from about 0 weight-percent to about 10 weight-percent in the elastomer formulations. Curing agent can be present from about 0.1 weight-percent to about 10 weight-percent in the elastomer formulations. Suitable curing agents include, for example, organometallic catalysts (e.g., dibutyltin dilaurate, tris(dimethylamino)methylsilane; and ethyltriacetoxysilane, among others, as well as combinations thereof), which are well known in the art for promoting condensation reaction. The disclosed weight-percent of the aforementioned components provides a total amount of components summing to 100 weight-percent for neat formulations.
Example 9: Elastomer Formulation #102 To a container of 200 mL were added red iron oxide (22.5 v), modified silicone resin (2) (26.0 g), and ethyl silicate (1.25 g). The mixture was thoroughly mixed together followed by the addition of dibutyltin dilaurate (0.26 g). The material mixture was mixed, degassed, casted onto a Teflon mold, and left at room temperature for 24 hours to produce elastomer #102.
Example 10: Elastomer Formulation #104 A mixture of modified silicone resin (2) (22.5 g). modified silicone resin (ii) (4.0 g), iron oxide (22.0 g), and ethyl silicate (1.25 g) were thoroughly mixed together. The dibutyltin Date Recue/Date Received 2020-07-24 dilaurate (0.25 g) was added to the mixture thereafter, followed by thorough mixing, degassing, and casting. The sample was left at room temperature for 24 hours, producing the cured silicone elastomer #104.
Example 11: Exemplary Elastomer Formulations Exemplary elastomer formulations are presented in Table IV. These formulations were made using procedures similar to those described in Example 10.
Table IV. Exemplary Elastomer Formulations.' Formulation Starting Resin2 Starting Resin2 Iron oxide3 Ethyl Curinf # (% w/w) ( 70 w/w) (% w/w) silicate4 agent-(%) w/w) ("/0 w/w) , 102 52 (Resin (2)) 45 2.5 0.5 (a) 104 45 (Resin (2)) 8 (Resin (ii)) 44 2.5 0.5 (a) 105 46 (Resin (2)) 7 (Resin (i)) 44 2.5 0.5 (a) 106 49.5 (Resin (2)) 45 5 0.5 (a) 107 50.5 (Resin (2)) 45 4 0.5 (a) 108 49.5 (Resin (2)) 6 (Resin (i)) 44 0.5(a) 109 50 (Resin (2)) 45 5 (b) 110 1 59 (Rcsin (2)) 36 5 (b) 111 1 47 (Resin (2)) 5 (Resin (i)) 44 4 (b) 112 52.5 (Resin (1)) 45 2 r 0.5 (a) 113 49.5 (Resin (1)) 45 5 0.5 (a) 114 52 (Resin (1)) 45 2.5 i 0.5 (a) 115 6.55 (Resin (2)) 55.7 (Resin (i)) 27.11 1.96, 0.54 (a) 8.14(Si02) ' 116 24.7 (Resin (1)) 24.7 (Resin (1)) 43 (h02) 7.6 (c) 117 25.5 (Resin (1)) 25.5 (Resin (1)) 43 6 (c) 118 49.5 (Resin (1)) 42.5 0.5 (a), 7.5 (c) 119 62.95 (Resin 34.55 2.5 (c) (1)) 120 73.5 (Resin (1)) 25 1.5 (b) 121 32.25 (Resin 32.25 (Resin (1)) 33 2.5 (b) (1)) 122 32 (Resin (1)) 32 (Resin (1)) 33 (TiO2) 3 (b) 123 29 (Resin (1)) 29 (Resin (1)) 27, 12 3 (c) (TiO2) 124 61 (Resin (2)) 24, 12 3 (b) (TiO2) 125 58.5 (Resin (2)) 36 (TiO2) 5 0.5 (a) 126 58.5 (Resin (2)) 24, 12 5 0.5 (a) (TiO2) Date Re9ue/Date Received 2020-07-24 'Numerical values represent weight-percent contribution of component to elastomer formulation.
2Starting resin(s) correspond to those resins having the structure presented in Tables I and III.
31ron oxide at the weight-percent contribution in the elastomer formulation is presented. When TiO2 replaces the iron oxide in the elastomer formulation, then only the weight-percent contribution of TiO2 is presented (e.g., Formulations 116, 122 and 125).When TiO2 supplements the iron oxide in the elastomer formulation, then the first weight-percent contribution reflects that of iron oxide and the second weight-percent contribution reflects that of TiO2 (e.g., Foimulations 123, 124 and 126).
4Ethyl silicate at the weight-percent contribution in the elastomer formulation is presented.
When SiO2 supplements the ethyl silicate in the elastomer formulation, then the first weight-percent contribution reflects that of ethyl silicate and the second weight-percent contribution reflects that of SiO2 (e.g., Formulation 115).
5Curing agents: a - dibutyltin dilaurate; b - tris(dimethylamino)methylsilane;
c-ethyltriacetoxysilane The performance attributes of select elastomer formulations comprising a modified silicone resin(s) are presented in Table V. As can be seen from Table V, the mechanical properties of the resultant formulations that include the modified silicone resins of Formula (I), Formula (II), or Formula (I) + Formula (I1), remain robust even after extensive aging at 316 C.
[01] Table V. Properties of Exemplary Elastomer Formulations.
[Formulations As-Prepared samples Samples after aging in 316 C
# Elongation Tensile Hours in Elongation Tensile (4)/0, RT) Strength 316 C (%, RT) Strength (MPa, RT) (MPa, RT) 102 142.8 3.4 2014 5.32 6.95 104 238.1 1.96 2014 12.6 6.79 112 79.1 1.55 2013 5.0 4.0 113 104.2 3.99 2011 12.3 5.48 114 122.1 3.30 2011 45.0 2.37 115 56.7 1.52 2011 5.8 3.68 116 205 12.06 2009 10.9 5.2 117 23.4 1.72 2009 23.4 2.64 118 15.2 1.19 2009 30.7 3.63 119 832.6 11.5 2009 8.36 4.64 120 208.2 2.7 2009 6.24 3.38 121 262.4 5.35 1000 46.7 4.33 122 291.6 11.2 2017 11.7 1.5 Date Recue/Date Received 2020-07-24 Formulations As-Prepared samples Samples after aging in 316 C
Elongation Tensile Hours in Elongation Tensile (%, RT) Strength 316 C (%, RT) Strength (MPa, RT) (MPa, RT) 123 218.8 4.1 2017 10.7 4.64 124 211.1 4.28 2017 1.2 2.4 125 140.3 6.22 2011 6.23 4.19 126 142.3 3.92 2011 3.2 7.2 Elastomer formulation applications The elastomer formulations that include a modified silicone resin(s) of Formula (I), Formula (II), or Formula (I) in combination with Formula (II), are amenable to industrial .. applications that require elastomer performance under high temperature conditions. These applications include use of the elastomer formulations for coatings, sealants, and gap-filling measures, among others.
While the present disclosure has been described with reference to certain embodiments, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted without departing from the scope of the present disclosure. In addition, modifications may be made to adapt a particular situation or material to the teachings of the present disclosure without departing from its scope.
Therefore, it is intended that the present disclosure not be limited to the particular embodiment disclosed, but that the present disclosure will include all embodiments falling within the scope of the .. appended claims.
Different aspects, embodiments and features are defined in detail herein. Each aspect, embodiment or feature so defined may be combined with any other aspect(s), embodiment(s) or feature(s) unless clearly indicated to the contrary.

Date Recue/Date Received 2020-07-24

Claims (37)

EMBODIMENTS IN WHICH AN EXCLUSIVE PROPERTY OR PRIVILEGE IS
CLAIMED ARE DEFINED AS FOLLOWS:

1. A modified silicone resin that is the reaction product of:
R8 Ri0 HO-Si- X-Si-OH HO ( Si 0 ________________________________ H
Ril R7 and wherein each of R6, R7, R8, R9, R19, and RH is independently selected from the group consisting of H, alkyl, alkenyl, alkynyl, and aryl;

wherein X is an inorganic oxide, wherein the inorganic oxide is:
a cyclosiloxane, wherein the cyclosiloxane is not a silsesquioxane;

\
Ti wherein R21 and R22 are independently propoxy, butoxy or phenyl;

\
Zr wherein R23 and R24 are independently propoxy, butoxy or phenyl; or 1 5 , wherein R25 is propoxy, butoxy or phenyl; and y ranges from 1 to 200.

2. The modified silicone resin of claim 1, wherein R6, R7, R8, R9, R19, and RH are each 20 independently H, C1-8 alkyl, C2_8 alkenyl, C2_8 alkynyl, or aryl.

Date Recue/Date Received 2021-09-01

3. The modified silicone resin of claim 1, wherein R6, R7, R8, R9, Rim, and RH are each independently methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl, or aryl.

4. The modified silicone resin of claim 1, wherein R6, R7, R8, R9, Rim, and RH are each independently methyl or phenyl.

5. The modified silicone resin of claim 1, wherein R6, R7, R8, R9, Rim, and RH are each independently H or alkyl.

6. The modified silicone resin of any one of claims 1 to 5, wherein the elastomer is further the reaction product of:

'I /
¨S ¨14, \
R1: , wherein each of R12 and R13 is independently selected from 1 5 the group consisting of H, alkyl, alkenyl, alkynyl, and aryl.

7. The modified silicone resin of claim 6, wherein R12 and R13 are each independently H, Ci_

8 alkyl, C2_8 alkenyl, C2_8 alkynyl, or aryl.
20 8. The modified silicone resin of claim 6, wherein R12 and R13 are each independently methyl, ethyl, propyl, butyl, ethylenyl, propylenyl, butylenyl, acetylenyl, diacetylenyl, or aryl.

9. The modified silicone resin of claim 6, wherein R12 and R13 are each independently methyl or phenyl.

10. The modified silicone resin of claim 6, wherein R12 and R13 are each independently H or alkyl.

Date Recue/Date Received 2021-09-01

11. The modified silicone resin of any one of claims 6 to 10, wherein the elastomer has a viscosity ranging from about 500 cSt to about 10,000 cSt.

12. The modified silicone resin of any one of claims 1 to 11, wherein the inorganic oxide is selected from the group consisting of:

\Z( ¨10/ \O¨, wherein R23 and R24 are propoxy;

\/
Ti HO/ \OH
, wherein R21 and R22 are butoxy;

, wherein R25 is phenyl;

Si ===õ, Si do (34 R47 R45 , wherein R4548 are methyl; and 1.
\ /R5 R53 ¨SI\ID
\
R51¨'"¨s-' R54 R52 , wherein R49-54 are methyl.

13. A method of forming modified silicone resin, the method comprising forming a reaction mixture by:
1 5 introducing into a reaction vessel a compound represented by formula (A):

Date Recue/Date Received 2021-09-01 R8 R i 0 X¨S

(A), and introducing into the reaction vessel a compound represented by formula (D):
HO ( Si 0 ________________________________ H

(D), wherein each of R6, R7, R8, R9, R10, and R11 is independently selected from the group consisting of H, alkyl, alkenyl, alkynyl, and aryl;
wherein X is an inorganic oxide, wherein the inorganic oxide is:
1 0 a cyclosiloxane, wherein the cyclosiloxane is not a silsesquioxane;

\
Ti HO/ \O¨, wherein R21 and R22 are independently propoxy, butoxy or phenyl;

zr wherein R23 and R24 are independently propoxy, butoxy or phenyl; or B\
, wherein R25 is propoxy, butoxy or phenyl; and 1 5 y ranges from 1 to 200.

14. The method of claim 13, wherein each of R6, R7, R8, R9, R10, and RH
is independently H
or alkyl.
Date Recue/Date Received 2021-09-01

15. The method of claim 13 or 14, further comprising:
introducing into the reaction vessel a compound represented by formula (B):

R (B), wherein each of R12 and R13 is independently selected from the group consisting of H, alkyl, alkenyl, alkynyl, and aryl; and 1 0 obtaining a compound represented by formula (II):
R6/7 R6 R8 Rlo R6 R6 I \ \
HO Si __________________ 0 Si 0 Si X Si 0 Si 0 Si OH
, R7" R7 R9F11R7/t R7 1Y 1Z
(II) wherein t ranges from 1 to 10, y ranges from 1 to 200 and z ranges from 1 to 1,000.

16. The method of claim 15, wherein each of R12 and R13 is independently H
or alkyl.

17. The method of claim 15 or 16, further comprising curing the compound represented by formula (II) for a time period of from about 30 minutes to about 2 days.

18. The method of claim 17, further comprising mixing a curing agent and a metal oxide with the compound represented by formula (II) to form an elastomer formulation.

Date Recue/Date Received 2021-09-01

19. The method of any one of claims 13 to 18, wherein the inorganic oxide is selected from the group consisting of:

\z( wherein R23 and R24 are propoxy;

\Ti/
, wherein R21 and R22 are butoxy;

(2)/ ¨
, wherein R25 is phenyl;

S I

Si OO
R47 R48 , wherein R45-48 are methyl; and R53 ./

\ \Of Si 0 R51--.'"¨s-' R54 R52 , wherein R49-54 are methyl.

20. The method of any one of claims 13 to 19, wherein the reaction vessel further comprises a solvent, wherein the solvent is toluene, benzene, tetrahydrofuran, acetonitrile, or N, N-dimethylformamide.

21. The method of any one of claims 13 to 19, wherein the reaction vessel further comprises a solvent, wherein the solvent is toluene.

22. The method of claim 20 or 21, wherein the reaction mixture is heated at a temperature of from about 80 C to about 140 C.

Date Recue/Date Received 2021-09-01

23. The method of claim 20 or 21, wherein the reaction mixture is heated at about 110 C
under inert atmosphere.

24. An elastomer fonnulation comprising a modified silicone resin as defined in any one of claims 1 to 12 and at least one metal oxide.

25. The elastomer formulation of claim 24, wherein the at least one metal oxide comprises Fe0, Fe203, Fe304, Ti02, Ce02, ZnO, Zr02, or any combination thereof.

26. The elastomer formulation of claim 24, wherein the at least one metal oxide comprises Fe0, Fe203, Fe304, Ti02, or any combination thereof.

27. The elastomer formulation of claim 24, 25, or 26, wherein the at least one metal oxide has a particle diameter size ranging from about 1 nm to about 5 gm.

28. The elastomer formulation of claim 24, 25, or 26, wherein the at least one metal oxide has a particle diameter size from about 25 nm to about 2 gm.

29. The elastomer formulation of claim 24, 25, or 26, wherein the at least one metal oxide has a particle diameter size from about 50 nm to about 500 nm.

30. The elastomer formulation of any one of claims 24 to 29, further comprising at least one curing agent.

31. The elastomer formulation of claim 30, wherein the at least one curing agent is at least one of dibutyltin dilaurate, tris(dimethylamino)methylsilane, and ethyltriacetoxysilane.

32. The elastomer formulation of claim 30, wherein the at least one curing agent is dibutyltin dilaurate.

Date Recue/Date Received 2021-09-01

33. The elastomer formulation of any one of claims 30, 31, or 32, wherein:
the at least one modified silicone resin is present in an amount ranging from about weight-percent to about 95 weight-percent;

the at least one metal oxide is present in an amount ranging from about 2 weight-percent to about 80 weight-percent; and the at least one curing agent is present in an amount ranging from about 0.10 weight-percent to about 10 weight-percent.

34. The elastomer formulation of any one of claims 24 to 33, further comprising at least one silicate.

35. The elastomer formulation of claim 34, wherein the at least one silicate comprises at least one of ethyl silicate, methyl silicate, isopropyl silicate and butyl silicate.

36. The elastomer formulation of any one of claims 24 to 35, further comprising at least one silica.

37. The elastomer formulation of claim 36, wherein the at least one silica comprises at least one of fumed silica and functionalized silica.

Date Recue/Date Received 2021-09-01